Production Process Engineer

Medstrom Ltd; Hemington; On-site; GBP 43,000 - 53,000; Full time

Benefits offered by this job

Contributory pension scheme

33 days’ annual leave

Discounts and cashback on shopping, S%

Salary Sacrifice Scheme: Cycle to Work

Training, support and mentorship

Birthday gift

Death in Service

Employee Ownership Trust (EOT)

Job summary

Medstrom Ltd in Castle Donington (employee-owned) is seeking a Production Process Engineer to lead lean improvements in our medical equipment assembly lines. You will own the continuous improvement roadmap, drive safety, quality and efficiency, and partner with Production, Quality, Supply Chain and R&D to deliver measurable gains.

You will apply 5S, Kaizen and Value Stream Mapping, write work instructions and SOPs, and mentor operators to embed world‑class manufacturing practices while

Qualifications

• 10 years’ experience as a Process Engineer or Manufacturing Engineer in a manufacturing environment.
• Experience in assembly manufacturing, preferably medical devices.
• Proven Lean Manufacturing implementation delivering measurable improvements.
• Knowledge of Lean tools: 5S, Kaizen, Value Stream Mapping, Standard Work, RCA.
• Proven track record of reducing waste, improving productivity and quality.
• Strong problem-solving, analytical and communication skills.
• Ability to influence change across departments.
• Engineering qualification (HNC/HND or Degree).
• Experience in regulated manufacturing (medical devices).
• Knowledge of PFMEA and Control Plans.

Responsibilities

• Lead continuous improvement initiatives across manufacturing and implement Lean tools.
• Identify opportunities to improve safety, quality, productivity, efficiency and cost.
• Develop and maintain manufacturing documentation, work instructions and SOPs.
• Collaborate with Production, Quality, Supply Chain and R&D for manufacturability and improvements.
• Investigate production issues, identify root causes and implement corrective actions.
• Collaborate with Quality and R&D on product issues and root-cause analysis.
• Monitor production data and KPIs; perform time studies, line balancing and capacity analysis.
• Write tooling specifications and work with R&D on jig design.
• Support engineering changes, product updates and transfers into manufacturing.
• Support cost reduction projects while maintaining quality and safety.
• Provide training to operators and team leaders.

Skills

Lean manufacturing

5S

Kaizen

Value Stream Mapping

Standard Work

Root Cause Analysis

Problem solving

Communication

Cross-functional collaboration

Education

HNC/HND or Degree

Tools

PFMEA

Control Plans

Job description

Are you passionate about continuous improvement and process efficiency? Do you want to play a key role in helping a growing employee-owned manufacturing business achieve its lean, quality and productivity goals?

We are looking for an experienced Production Process Engineer to join our manufacturing team in Castle Donington, specialising in the assembly of medical equipment. This is a practical role for someone who is passionate about continuous improvement, lean manufacturing and developing efficient, world-class production processes.

The successful candidate will take ownership of the continuous improvement roadmap for production, proactively identifying opportunities to improve safety, quality, productivity, efficiency and cost. We are looking for someone who challenges existing ways of working, brings fresh ideas, and delivers measurable improvements rather than simply maintaining current processes.

The Benefits

• Starting salary in the region of £48,000, depending on experience
• Contributory pension scheme
• 33 days’ annual leave entitlement
• Discounts and cashback on shopping, supermarkets, and holidays
• Salary Sacrifice Schemes, including Cycle to Work
• Great training, support and mentorship
• Birthday gift
• Death in Service benefit provided
• Be a part of an Employee Ownership Trust (EOT) and the associated benefits of having a stake in the company

The Role

Your main responsibilities will be:

• Lead and own continuous improvement initiatives across the manufacturing operation and implement Lean Manufacturing tools, including 5S, Kaizen, Standard Work, Visual Management and Value Stream Mapping
• Proactively identify opportunities to improve safety, quality, productivity, efficiency and cost
• Develop and maintain manufacturing documentation, work instructions and standard operating procedures
• Work closely with Production, Quality, Supply Chain and R&D to ensure products are designed for efficient manufacture and existing products continue to be improved
• Investigate production issues, identify root causes and implement permanent corrective actions
• Collaborate with Quality and R&D in the investigation of product issues, identification of root causes and implementation of permanent corrective actions
• Monitor production data and KPIs to identify trends and drive measurable improvements; carry out time studies, line balancing and capacity analysis
• Write specifications for tooling and production jigs and work closely with R&D on the design of these
• Support engineering changes, product updates and design transfers into manufacturing
• Support cost reduction projects, maintaining product quality and safety
• Provide training to operators and team leaders

Hours of Work: 37.5 per week, Monday - Friday, 8am - 4pm.

About You

• Minimum 10 years’ experience as a Process Engineer or Manufacturing Engineer within a manufacturing environment
• Significant experience in an assembly manufacturing environment, preferably within the medical device or medical equipment industry
• Proven experience implementing Lean Manufacturing principles and delivering measurable continuous improvement projects
• Strong knowledge of Lean tools such as 5S, Kaizen, Value Stream Mapping, Standard Work and Root Cause Analysis
• Demonstrable success in improving production lines, reducing waste, increasing productivity and improving quality
• Excellent problem-solving, analytical and communication skills
• Ability to influence change and work collaboratively across multiple departments
• Engineering qualification (HNC/HND or Degree) or equivalent industry experience
• Experience working within a regulated manufacturing environment (e.g. medical devices)
• Knowledge of PFMEA, Control Plans or similar quality improvement tools

The recruitment process will consist of at least two interview stages, both of which will require attendance on site.

Candidates who progress to the final stage will be invited to complete either a practical assessment or a presentation, with the format to be confirmed prior to the final interview.

Why Join Medstrom?

Established in 2010, Medstrom has grown substantially through its commitment to supporting healthcare providers with innovative products and services that improve patient outcomes. Despite significant growth, we have maintained an open, collaborative culture where employees are empowered to contribute and make a difference.

As an Employee Ownership Trust, every employee shares in our success, creating a business where everyone has a genuine stake in the future.

Webrecruit and Medstrom are equal opportunities employers, value diversity and are strongly committed to providing equal employment opportunities for all employees and all applicants for employment. Equal opportunities are the only acceptable way to conduct business and we believe that the more inclusive our environments are, the better our work will be.